Data / Medical devices / Powder, Porcelain / South Korea
FDA-registered makers of Powder, Porcelain in South Korea: 16 establishments
16 establishments in South Korea are registered with the FDA to make Powder, Porcelain (product code EIH). 15 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Powder, Porcelain
- Product code
- EIH
- Country
- South Korea
Makers of Powder, Porcelain in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| GENOSS Co., Ltd. | Suwon-si Gyeonggi, South Korea | Manufacturer | 10 | June 21, 2024 | 0 | 0 | 0 | api.fda.gov |
| Vatech mcis Co., Ltd. | Suwon-si Gyeonggi, South Korea | Manufacturer | 5 | June 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| ARUM DENTISTRY Co., Ltd. | Yuseong-gu Daejeon, South Korea | Manufacturer | 3 | July 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Dentalmax Co., Ltd | Cheonan-si Chungnam, South Korea | Manufacturer | 3 | September 30, 2024 | 0 | 0 | 0 | api.fda.gov |
| DMAX Co., Ltd. | Daegu, South Korea | Contract manufacturer, Manufacturer | 3 | June 12, 2025 | 0 | 0 | 0 | api.fda.gov |
| Hass Corp. | Gangneung-si Gangwon, South Korea | Manufacturer | 3 | June 11, 2026 | 0 | 0 | 0 | api.fda.gov |
| Hass Corp. | Gangneung-si Gangwon, South Korea | Manufacturer | 3 | June 11, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ids Korea | Seoul, South Korea | Manufacturer | 2 | October 11, 2019 | 0 | 0 | 0 | api.fda.gov |
| Osstem Implant Co., Ltd. | Gangseo-gu Seoul, South Korea | Specification developer | 2 | November 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Osstem Implant Co., Ltd. | SIHEUNG Gyeonggi, South Korea | Manufacturer | 2 | November 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Doctus Global | Goyang-si, Gyeonggi-do, South Korea | Manufacturer | 1 | June 30, 2023 | 0 | 0 | 0 | api.fda.gov |
| Mediclus Co., Ltd | Cheongju-si Chungbuk, South Korea | Manufacturer | 1 | August 21, 2026 | 0 | 0 | 0 | api.fda.gov |
| SMD Dental Laboratory | Heungdeok-gu Cheongju-si Chungbuk, South Korea | Manufacturer | 1 | October 31, 2018 | 0 | 0 | 0 | api.fda.gov |
| U&c International Co., Ltd. | Ansan-si Gyeonggi, South Korea | Manufacturer | 1 | October 11, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vericom Co., Ltd. | Chuncheon-Si Gangwon, South Korea | Manufacturer | 1 | July 1, 2021 | 0 | 0 | 0 | api.fda.gov |
| Amskorea Co.,ltd | Goyang-si Gyeonggi, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.